1.Congenital Adrenal Hyperplasia in Korea.
Journal of Korean Society of Pediatric Endocrinology 2005;10(2):132-137
No abstract available.
Adrenal Hyperplasia, Congenital*
;
Korea*
3.A Study on the ticks of Chejudo IV. Monthly life flow of ticks.
The Korean Journal of Parasitology 1973;11(2):95-101
Following is the result of a survey hold over a two year period(1971-1972), on the appearence and disappearence of ticks on cattle in Cheju. Number of Haemaphysalis longicornis. Larvae: From the beginning of July to mid September larvae abounded reaching their peak during July and August. In 1971 their period was from July to September. In 1972 their period was from May to October. In both years their number reached their highest point in July and August(Table 1.2) Nymph: Ticks were found from February to October(1971) and January to December (1972), and they were especially plentiful during the periods of may (1971)(Table 1.2). Adult : Ticks were in evidence from April to October(1971) and January to December(1972). They were especially plentiful during the periods of July and August(1971) and August(1972). However, in 1972 they were also quite plentiful in June and July(1972)(Table 1.2). Percentage of Haemaphysalis longicornis. 1971(Fig. 1): February-May: nymph 94.1 percent, adult female 5.9 percent ; July-August: larvae 54.8 percent, 1972(Fig. 2) : January-May: larvae 18.2 percent, nymph 18.2 percent, adult female 3.8 percent; July-August: larvae 48.2 percent, nymph 11.6 percent, adult female 40.2 percent. Number of Boophilus microplus: larvae; Ticks were in evidence from April to October(1971) and January to December(1972). They were especially plentiful during the periods of June adn July(1971) and July to August(1972). However, in 1972 they were also quite plentiful in May. Nymph: Ticks were in evidence from January to December 1971 and 1972. They were especially plentiful during the periods of June and August(1971) and May to September(1972). However, in 1972 they were also quite plentiful in October and November. Adult: Ticks were in evidence from January to December 1971 and 1972. They were especially plentiful during the periods of July to September(1971) and July (1972). However, in 1972 they were also quite plentiful in May to August. Percentage of Boophilus microplus. 1971(Fig. 3): January-May: larvae 40.3 percent, nymph 32.3 percent, adult female 27.1 percent, July-August: larvae 31.2 percent , nymph 35.7 percent, adult female 33.5 percent. 1972(Fig. 4): January-May: larvae 32.8 percent , nymph 42.1 percent, adult female 25.1 percent, July-August: larvae 44.2 percent, nymph 26.4 percent, adult female 29.4 percent.
parasitology-arthropoda-tick
;
Haemaphysalis longicornis
;
Boophilus microplus
;
biology
4.Sexual Precocity.
Journal of the Korean Pediatric Society 2003;46(Suppl 3):S400-S410
No abstract available.
5.Management of Childhood Hyperthyroidism.
Journal of Korean Society of Pediatric Endocrinology 1999;4(1):10-13
No abstract available.
Hyperthyroidism*
6.Nesidioblastosis in Neonate with Persistent Hyperinsulinemic Hypoglycemia.
Il Tae WHANG ; Ho Seong KIM ; Ho Seong HAN
Journal of Korean Society of Pediatric Endocrinology 1998;3(2):231-236
Nesidioblastosis, also known as persistent hyperinsulinemic hypoglycemia of infancy(PHHI) or familial hyperinsulinsm, is the most common cause of recurrent severe hypoglycemia in infancy. It is an autosomal recessive disorder characterized by irregular insulin secretion leading to inappropriately raised plasma insulin concentration compared to blood glucose levels. Recently, mutations in the sulfonylurea receptor(SUR) have been described in association with PHHI. The mainstay of medical treatment is glucose infusion and diazoxide or long acting somatostatin. If medical treatment fails in preventing hypoglycemia, near total pancreatectomy is recommended. We report one case of nesidioblastosis cured by near total pancreatectomy with brief review of literatures.
Blood Glucose
;
Congenital Hyperinsulinism*
;
Diazoxide
;
Glucose
;
Humans
;
Hypoglycemia
;
Infant, Newborn*
;
Insulin
;
Nesidioblastosis*
;
Pancreatectomy
;
Plasma
;
Somatostatin
7.Growth pattern and final height in congenital adrenal hyperplasia.
Journal of the Korean Pediatric Society 1993;36(10):1359-1365
Clinical characteristics and growth pattern were evaluated in 42 patients with classical congenital adrenal hyperplasia treated since diagnosis. And final height was evaluated in 16 patients who had reached final adult height with regard to clincal form, degree of hormonal control, and age of initial treatment. The results were as follows; 1) Among 42 patients with classical congenital adrenal hyperplasia, the male to female sex ratio was 1:1.8 (15 males and 27 females), and the frequency of the salt-wasting form (SW) and simple virilizing form (SV) was same (21 SW and 21 SV). 2) The length of time to initial treatment averated 4.2 months (range: 9 days-49 months) for salt-wasting form and 8.8 years (range: 1 month-21 years) for simple virilizing form. 3) In seven cases, precocious puberty developed during treatment and the average age on development was 6.8 years for salt-wasting form and 5.4 years for simple virilzing form. 4) The pattern of growth from birth throughout childhood in salt-wasting patients showed poor growth initially. The average height in simple virilizing patients was above the mean in the first years of life, declining steadily (falling below the mean by age 12), until the end of the growt period. 5) Bone ages were retarded initially in salt-wasting patients, thereafter accelerating by age 3, meanwhile in simple virilizing patients advanced initially. 6) In 16 patients who had reached final adult height, analysis of final height with regard to clinical form, degree of hormonal control, and age of initial treatment indicated that neither of them seem to after the height outcome. In conclusion, classical congenital adrenal hyperplasia patients seem to achieve final height consistently below the mean for the general population. Factors to affect the height outcome (clinical form, degree of hormonal control, age of initial treatment) may influence concomitently, and another factor may be present.
Adrenal Hyperplasia, Congenital*
;
Adult
;
Diagnosis
;
Female
;
Humans
;
Male
;
Parturition
;
Puberty, Precocious
;
Sex Ratio
8.A Case of 5 alpha-reductase Deficiency in Infancy.
Journal of Korean Society of Pediatric Endocrinology 1998;3(1):96-101
5 alpha-reductase deficiency resulting in male pseudohermaphroditism is a rare disease characterized by clitoral-like phallus, bifid scrotum, urogenital sinus, testis cited in labioscrotal folds. Evaluation of plasma T/DHT ratios in infancy, particularly after hCG stimulation of the testes and elevated urinary tetrahydrocortisol (THF) to 5 alpha-tetrahydrocortisol(5 alpha-THF) ratios provide a valuable dianostic test for 5 alpha-reductase deficiency. We report one case of 5 alpha-reductase deficiency who were presented with ambiguous genitalia and elevated T/DHT ratio before and after hCG stimulation.
46, XY Disorders of Sex Development
;
Cholestenone 5 alpha-Reductase*
;
Disorders of Sex Development
;
Plasma
;
Rare Diseases
;
Scrotum
;
Testis
;
Tetrahydrocortisol
9.The effects of phenobarbital on the sleep of some male young adults.
Journal of Korean Neuropsychiatric Association 1991;30(5):832-839
No abstract available.
Humans
;
Male*
;
Phenobarbital*
;
Young Adult*
10.The effects of phenobarbital on the sleep of some male young adults.
Journal of Korean Neuropsychiatric Association 1991;30(5):832-839
No abstract available.
Humans
;
Male*
;
Phenobarbital*
;
Young Adult*